HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49410Generated: October 30, 2026
Oxalic Acid → HCID 131724378, compound
https://huagongshe.com/reaction/49410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (7alpha,14beta,15beta,17alpha)-3-Methoxy-7-methyl-14,15-methyleneestra-2,5(10)-diene-17-methanol | HCID 69625019 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131724378 | HCID 131724378 | — |
Reaction Steps
A solution of (7α,14β,15β,17α)-3-methoxy-7-methyl-14,15-methyleneestra-2,5(10)-diene-17-methanol (Example 1, step vi; 7.38 g) in a mixture of methanol (68 ml) and tetrahydrofuran (48 ml) was treated with a solution of oxalic acid (2.38 g) in water (40 ml). After 1 h stirring at room temperature, the reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate and the product was extracted into ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Column chromatography afforded (7α,14β,15β,17α)-17-(hydroxyethyl)-7-methyl-14,15-methyleneestr-5(10)-en-3-one (4.27 g). 1H NMR (CDCl3) δ3.69 (m, 1H), 3.51 (t, 1H, J=9.0 Hz), 2.72 (bs, 2H), 2.46 (bs, 2H), 1.04 (s, 3H), 0.69 (d, 3H, J=7.1 Hz), 0.48(dd, 1H, J=8.3 and 5.1 Hz), 0.27 (dd, 1H, J=5.1 and 3.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706700B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-d3ce938e8ba948cdb819560530d83ab7 |
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| Source note | uspto-grants-2004_03 |
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